反应详情

To 262 mg (1.05 mmol) decyloxyaniline (Salor) in 5 ml ethanol, 0.26 ml HCl/dioxane 4N is added, the mixture stirred for 3 min, and then 256 mg (1.00 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine (Example 67A.1) is added. After 2 h boiling under reflux, the mixture is cooled and concentrated by evaporation. The residue is stirred with 6 ml NH3 solution (10% in water or 10 ml sat. NaHCO3 solution) and 15 ml dichloromethane/methanol 50:1 for 30 min. The aqueous phase is then separated off and extracted again with dichloromethane. The organic phase is dried (Na2SO4) and concentrated by evaporation. Crystallization [possibly after chromatography on SiO2 (ethyl acetate/CH3OH, 19:1)] from acetonitrile (or methanol) yields the title compound: m.p.: 116-119° C.; Anal. calc.(C30H36N4O) C, 76.89%; H, 7.74%; N, 11.96%. found C, 76.7%; H, 7.7%; N, 11.9%; FAB MS (M+H)+=469.

1. waitAfter 2 h boiling
2. temperatureunder reflux
3. temperaturethe mixture is cooled
4. concentrationconcentrated by evaporation
5. stirringThe residue is stirred with 6 ml NH3 solution (10% in water or 10 ml sat. NaHCO3 solution) and 15 ml dichloromethane/methanol 50:1 for 30 min
6. customThe aqueous phase is then separated off
7. extractionextracted again with dichloromethane
8. dry with materialThe organic phase is dried (Na2SO4)
9. concentrationconcentrated by evaporation
10. customCrystallization [possibly after chromatography on SiO2 (ethyl acetate/CH3OH, 19:1)] from acetonitrile (or methanol)